Team:Oxford/protocols/QIAquick Gel Extraction
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- | + | <!--this will number your steps 1,2,3,etc--> | |
+ | <ol style="list-style-type:decimal;"> | ||
+ | <li>After growing cell cutlers overnight in LB, resuspend pelleted cells in 250 μl Buffer P1 and transfer it into a microcentrifuge tube.<BR><BR> | ||
+ | <li>Add 250 μl of Buffer P2 and mix by inverting the tube 6 times. The cell suspension should turn blue.<BR><BR> | ||
+ | <li>Add 350 μl of Buffer N3 and mix the suspension immediately by inverting 6 times.<BR><BR> | ||
+ | <li>Centrifuge for 10 minutes at 13000 rpm (or 17900 x g). Apply the supernatants to a spin colums<BR><BR> | ||
+ | <li>Centrifuge again for 30-60 seconds and discard the flow-through.<BR><BR> | ||
+ | <li> Wash the spin column by adding 500 μl of the PB buffer and centrifuge for 30-60s.<BR><BR> | ||
+ | <li>Discard the flow-through and wash the spin column again by adding 750 uL of PE buffer. Centrifuge for 1 minute.<BR><BR> | ||
+ | <li>Discard the flow-through and centrifuge again for 1 minute. Now place the column in a 1.5ml microcentrifuge tube.<BR><BR> | ||
+ | <li>Add 50 μl of the EB buffer to the centre of the spin column. Let stand for 2 minutes and centrifuge for 1 minute.<BR><BR> | ||
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Revision as of 13:33, 23 July 2014
QIAquick Gel Extraction
↩ Back to other protocols.
- After growing cell cutlers overnight in LB, resuspend pelleted cells in 250 μl Buffer P1 and transfer it into a microcentrifuge tube.
- Add 250 μl of Buffer P2 and mix by inverting the tube 6 times. The cell suspension should turn blue.
- Add 350 μl of Buffer N3 and mix the suspension immediately by inverting 6 times.
- Centrifuge for 10 minutes at 13000 rpm (or 17900 x g). Apply the supernatants to a spin colums
- Centrifuge again for 30-60 seconds and discard the flow-through.
- Wash the spin column by adding 500 μl of the PB buffer and centrifuge for 30-60s.
- Discard the flow-through and wash the spin column again by adding 750 uL of PE buffer. Centrifuge for 1 minute.
- Discard the flow-through and centrifuge again for 1 minute. Now place the column in a 1.5ml microcentrifuge tube.
- Add 50 μl of the EB buffer to the centre of the spin column. Let stand for 2 minutes and centrifuge for 1 minute.